Evidence map›Paper›PMID 38002740›Full record

ArticleJournal of clinical medicine2023

«Digesting Crohn's Disease»: The Journey of Young Adults since Diagnosis.

Nathalie Touma, Louise Zanni, Pierre Blanc, Guillaume Savoye, Carolina Baeza-Velasco

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Nathalie ToumaLaboratoire de Psychopathologie et Processus de Santé, Université Paris Cité, 92100 Boulogne-Billancourt, France.ORCID 0000-0003-2106-5906
Louise ZanniLaboratoire de Psychopathologie et Processus de Santé, Université Paris Cité, 92100 Boulogne-Billancourt, France.ORCID 0009-0005-7696-2307
Pierre BlancService d'Hépato-Gastroentérologie B, Centre Hospitalier Universitaire de Montpellier, 371 Av. du Doyen Gaston Giraud, 34090 Montpellier, France.
Guillaume SavoyeService d'Hépato-Gastroentérologie, Centre Hospitalier Universitaire de Rouen, Université de Rouen Normandie, UMR 1073, 76000 Rouen, France.
Carolina Baeza-VelascoLaboratoire de Psychopathologie et Processus de Santé, Université Paris Cité, 92100 Boulogne-Billancourt, France.ORCID 0000-0002-3279-8366
Université Paris Cité · FRCentre Hospitalier Universitaire de Montpellier · FRInstitute for Research and Innovation in Biomedicine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Crohn's disease affects 2.5 million people in Europe (more than 100,000 people in France) and often occurs between the ages of 15 and 30, a period marked by self-construction. However, few studies have focused on the experience of the diagnosis during this sensitive developmental stage. This study aimed to qualitatively explore the experience of Crohn's disease in young adults since their diagnosis. Fifteen young adults (18-35 years) diagnosed with Crohn's disease participated in a semi-directive interview. Narrative data were subjected to a thematic analysis, and thirty percent of the interviews were double-coded. The results revealed an evolution of four main themes since diagnosis: (1) course of care, (2) illness perceptions, (3) disease management and (4) self-perception. For most participants, the onset of the disease was difficult, marked by severe symptoms requiring hospitalization, numerous medical examinations and sometimes several consultations before diagnosis. This journey was more difficult when it was associated with negative relations with the medical staff, who were sometimes perceived as unsupportive. Thus, some people described this diagnostic period as an "ordeal", while others experienced it as a "relief" from their suffering. The announcement of the diagnosis was often a "shock", an "upheaval" or a "downfall", followed by phases of denial associated with a desire to maintain a "normal life" and not to be defined by the disease. Despite a difficult start, most participants grew from their experience with CD, with a sense of a personal development that was made possible by self-regulation processes that enabled them to draw on their own experience and resources to adjust to their illness. By highlighting positive possibilities for evolution, this study suggests the importance of supporting the psychological resources of young adults by proposing, at an early stage, psychological support or therapies focused on acceptance and engagement.

Indexed as

Crohn’s diseaseemerging adultsillness identitypsychosocial adjustment to illnessyoung adults

Identifiers

PMID38002740
PMCPMC10672720
OpenAlexW4388722994

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.